Megacystis, mydriasis, and ion channel defect in mice lacking the α3 neuronal nicotinic acetylcholine receptor
Megacystis, mydriasis, and ion channel defect in mice lacking the α3 neuronal nicotinic acetylcholine receptor
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DOI:
10.1073/pnas.96.10.5746
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发表时间:
1999-05-11
影响因子:
11.1
通讯作者:
Beaudet, AL
中科院分区:
文献类型:
--
作者:
Xu, W;Gelber, S;Beaudet, AL
The alpha 3 subunit of the neuronal nicotinic acetylcholine receptor is widely expressed in autonomic ganglia and in some parts of the brain, The alpha 3 subunit can form heteromultimeric ion channels with other alpha subunits and with beta 2 and beta 4 subunits, but its function in vivo is poorly understood. We prepared a null mutation for the alpha 3 gene by deletion of exon 5 and found that homozygous (-/-) mice lacked detectable mRNA on Northern blotting, The -/- mice survive to birth but have impaired growth and increased mortality before and after weaning, The -/- mice have extreme bladder enlargement, dribbling urination, bladder infection, urinary stones, and widely dilated ocular pupils that do not contract in response to light, Detailed histological studies of -/- mice revealed no significant abnormalities in brain or peripheral tissues except urinary bladder, where inflammation was prominent. Ganglion cells and axons were present in bladder and bowel, Bladder strips from -/- mice failed to contract in response to 0.1 mPrl nicotine, but did contract in response to electrical field stimulation or carbamoylcholine, The number of acetylcholine-activated single-channel currents was severely reduced in the neurons of superior cervical ganglia in -/- mice with five physiologically distinguishable nicotinic acetylcholine receptor subtypes with different conductance and kinetic properties in wild-type mice, all of which were reduced in -/- mice. The findings in the alpha 3-null mice suggest that this subunit is an essential component of the nicotinic receptors mediating normal function of the autonomic nervous system. The phenotype in -/- mice may be similar to the rare human genetic disorder of megacystis-microcolon-intestinal hypoperistalsis syndrome.